Wouldn't the inductive effect be more prominent in ester than the acyl chloride since the electronegativity of oxygen is higher than the that of chloride? Because in this sense, I think acyl chloride should be placed in a lower wavenumber than ester....can anyone help me on this?!?
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Is there any way to quantify these effects
in 6:40 . I know that the resonance effect of -OR is more than the inductive effect. Please correct me.
I also know it...
Wouldn't the inductive effect be more prominent in ester than the acyl chloride since the electronegativity of oxygen is higher than the that of chloride? Because in this sense, I think acyl chloride should be placed in a lower wavenumber than ester....can anyone help me on this?!?
Exactly same doubt
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